let me share with you the incredible journey of Jameson Lee Trevino, a resilient, smart, beautiful baby boy who continues to inspire. On February 5, 2025, at my 20-week anatomy scan, we discovered that baby Jameson had severe hydrocephalus, with each ventricle in his brain measuring 24 mm bilaterally. But Jameson was determined to make his entrance, and on May 16, 2025, at just 36 weeks, he arrived. As we welcomed Jameson into the world, we also learned that he had additional genetic conditions, including underdeveloped left side of his body, fused hands, and a smaller left eyeball. Despite these challenges, Jameson's strength and spirit have been a beacon of hope. However, our journey has not been without its obstacles. Doctor Bowman at Children's Covenant NICU told me just two hours after my C-section, before I had even met my son, that I should consider comfort care, implying that Jameson's life may not have value. But I knew that Jameson was a fighter, and I advocated tirelessly for his right to receive the medical care he needed. Finally, after multiple battles with the doctors, they agreed to perform the life-changing VP shunt surgery. Today, Jameson continues to defy the odds, and we are committed to ensuring that he receives the best possible care. We have upcoming appointments with a hand orthopedic specialist at Cook's Children's, as well as with Scottish Rite, and we are reaching out for your support to help us get Jameson to Dallas for these critical appointments. Medicaid has refused to cover our housing and food expenses, citing that Jameson is not being hospitalized, so we are relying on the kindness of strangers to help us cover these essential costs. Can you please consider donating just $1 to help us get Jameson to Dallas and back, so that he can receive the care he so desperately needs? Your generosity will be a lifeline to our family, and we are forever grateful.
let me share with you the incredible journey of Jameson Lee Trevino, a resilient, smart, beautiful baby boy who continues to inspire. On February 5, 2025, at my 20-week anatomy scan, we discovered that baby Jameson had severe hydrocephalus, with each ventricle in his brain measuring 24 mm bilaterally. But Jameson was determined to make his entrance, and on May 16, 2025, at just 36 weeks, he arrived. As we welcomed Jameson into the world, we also learned that he had additional genetic conditions, including underdeveloped left side of his body, fused hands, and a smaller left eyeball. Despite these challenges, Jameson's strength and spirit have been a beacon of hope. However, our journey has not been without its obstacles. Doctor Bowman at Children's Covenant NICU told me just two hours after my C-section, before I had even met my son, that I should consider comfort care, implying that Jameson's life may not have value. But I knew that Jameson was a fighter, and I advocated tirelessly for his right to receive the medical care he needed. Finally, after multiple battles with the doctors, they agreed to perform the life-changing VP shunt surgery. Today, Jameson continues to defy the odds, and we are committed to ensuring that he receives the best possible care. We have upcoming appointments with a hand orthopedic specialist at Cook's Children's, as well as with Scottish Rite, and we are reaching out for your support to help us get Jameson to Dallas for these critical appointments. Medicaid has refused to cover our housing and food expenses, citing that Jameson is not being hospitalized, so we are relying on the kindness of strangers to help us cover these essential costs. Can you please consider donating just $1 to help us get Jameson to Dallas and back, so that he can receive the care he so desperately needs? Your generosity will be a lifeline to our family, and we are forever grateful.
